Skip to main content

dexmedetomidine (Dexdor®)

 

Following a full submission

AWMSG advice

Status: Recommended

Dexmedetomidine (Dexdor®) is recommended as an option for use within NHS Wales for the sedation of adult intensive care unit (ICU) patients requiring a sedation level not deeper than arousal in response to verbal stimulation (corresponding to Richmond Agitation-Sedation Scale [RASS] 0 to -3).

In June 2022 the marketing authorisation holder issued a direct healthcare professional communication (DHPC) to share important information regarding an increased risk of mortality in intensive care unit (ICU) patients ≤ 65 years. The SmPC has been updated with a warning statement. The full DHCP can be accessed here.

 Final Recommendation: dexmedetomidine (Dexdor) 661 (PDF, 259Kb)
 Appraisal Report: dexmedetomidine (Dexdor) 661 (PDF, 279Kb)

Medicine details

Medicine name dexmedetomidine (Dexdor®)
Formulation 100 micrograms/ml concentrate for solution for infusion
Reference number 661
Indication

Sedation of adult ICU (intensive care unit) patients requiring a sedation level not deeper than arousal in response to verbal stimulation (corresponding to Richmond Agitation-Sedation Scale (RASS) 0 to -3)

Company Orion Pharma (UK) Ltd
BNF chapter Anaesthesia
Submission type Full
Status Recommended
Advice number 2312
NMG meeting date 12/06/2012
AWMSG meeting date 18/07/2012
Ratification by Welsh Government 07/08/2012
Date of issue 13/08/2012
Date of last review 30/09/2016
Follow AWTTC: